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1W30

PyrR of Mycobacterium Tuberculosis as a potential drug target

1W30 の概要
エントリーDOI10.2210/pdb1w30/pdb
分子名称PYRR BIFUNCTIONAL PROTEIN (2 entities in total)
機能のキーワードpyrr, transferase, glycosyltransferase, psi, protein structure initiative, tb structural genomics consortium, tb, tbsgc
由来する生物種MYCOBACTERIUM TUBERCULOSIS
タンパク質・核酸の鎖数2
化学式量合計43259.19
構造登録者
主引用文献Kantardjieff, K.A.,Vasquez, C.,Castro, P.,Warfel, N.N.,Rho, B.-S.,Lekin, T.,Kim, C.-Y.,Segelke, B.W.,Terwilliger, T.,Rupp, B.
Structure of Pyrr (Rv1379) from Mycobacterium Tuberculosis: A Persistence Gene and Protein Drug Target
Acta Crystallogr.,Sect.D, 61:355-, 2005
Cited by
PubMed Abstract: The Mycobacterium tuberculosis pyrR gene (Rv1379) encodes a protein that regulates the expression of pyrimidine-nucleotide biosynthesis (pyr) genes in a UMP-dependent manner. Because pyrimidine biosynthesis is an essential step in the progression of TB, the gene product pyrR is an attractive antitubercular drug target. The 1.9 A native structure of Mtb pyrR determined by the TB Structural Genomics Consortium facilities in trigonal space group P3(1)21 is reported, with unit-cell parameters a = 66.64, c = 154.72 A at 120 K and two molecules in the asymmetric unit. The three-dimensional structure and residual uracil phosphoribosyltransferase activity point to a common PRTase ancestor for pyrR. However, while PRPP- and UMP-binding sites have been retained in Mtb pyrR, a distinct dimer interaction among subunits creates a deep positively charged cleft capable of binding pyr mRNA. In silico screening of pyrimidine-nucleoside analogs has revealed a number of potential lead compounds that, if bound to Mtb pyrR, could facilitate transcriptional attenuation, particularly cyclopentenyl nucleosides.
PubMed: 15805589
DOI: 10.1107/S090744490403389X
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.9 Å)
構造検証レポート
Validation report summary of 1w30
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-15に公開中

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